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CytoMicroArray High Resolution (CMA 750K) + FISH 21
CytoMicroArray High Resolution (CMA 750K) + FISH 21
CytoMicroarray is a DNA based test performed on Maniotic Fluid Sample (AF) to identify fetal chromosomal numerical abnormalities (aneuploidy), copy number variations or CNVs (>100Kb micro-deletions and micro-duplications), Loss of Heterozygosity (LOH) and Uniparental Disomy (UPD). Recommended by ACMG as first-tier test for ruling out aneuploidy in fetus. FISH 21 test is ordered in addition for a quick result to confirm or rule out Trisomy 21 (Down syndrome)
19500
₹2599
76% OFF
2 weeks
Schedule test now
Schedule test now
Sample Collection and Transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
AF CytoMicroArray + FISH 21, AF CMA 750K + FISH 21, AF CMA High Resolution + FISH 21
Specialities
ObGyn, IVF, Fetal Medicine
Technology
CMA: The Affymetrix Cytoscan 750K Array includes 750,000 CNV markers with 550,000 unique non polymorphic probes and around 200,000 SNPs. Clinically significant CNVs of >100Kb reported. Data is analysed using Chromosome analysis suite (ChAS) software and interpreted using bioinformatic predictor tools, research publications and ACMG guidelines. The test does not detect balanced chromosomal translocations , small indels and point mutations. FISH: DNA probes (small molecules of DNA that are designed to hybridise with a particular section of the genome) are used detect specific complementary sequences on a chromosome. It is undertaken in situ on chromosomes spread on a slide and visualised by microscopy.
Conditions & Symptoms
High risk screening (Double marker, Quadruple Marker or NIPT) results, high risk for aneuploidy, bad obstetric history, parents carriers of translocations, history of Trisomy 21 or Down syndrome baby or fetus, ultrasound markers
Additional Information
GeneTech pioneered genetic testing in India in 1998 and has the most comprehensive range of tests using technologies.
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IVF Success: The Role of GeneAndro and GeneFemina
Enhancing IVF Outcomes: GeneAndro and GeneFemina Explained
Unlocking IVF Potential with GeneAndro and GeneFemina
Achieving IVF Success: Insights on GeneAndro and GeneFemina
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Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy Amniocentesis is an ultrasound guided sterile proceedure performed by experienced radiologits to retrive 20-30ml of the amniotic fluid each from two dichorionic and diamniotic sacs. The fluid which contains fetal cells is used in the genetic lab to test for genetic abnormalities. It is done between 16-22 weeks of gestation. Amniocentesis proceedure is done at our central laboratory in Hyderabad. Prior appointment required. Call 9848041127 for details
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Test CatalogueCytoMicroArray High Resolution (CMA 750K) + FISH 21

Full Body Checkup - Essential in Hyderabad

Unlock insights into your health, ancestry, or future risks with our advanced genetic testing. Backed by cutting-edge science and expert guidance, Genetech helps you make informed decisions—personalized to your DNA.

₹1599
₹2599
76% OFF
2 weeks
Schedule test now

CytoMicroArray High Resolution (CMA 750K) + FISH 21

CytoMicroarray is a DNA based test performed on Maniotic Fluid Sample (AF) to identify fetal chromosomal numerical abnormalities (aneuploidy), copy number variations or CNVs (>100Kb micro-deletions and micro-duplications), Loss of Heterozygosity (LOH) and Uniparental Disomy (UPD). Recommended by ACMG as first-tier test for ruling out aneuploidy in fetus. FISH 21 test is ordered in addition for a quick result to confirm or rule out Trisomy 21 (Down syndrome)

19500
₹2599
76% OFF
2 weeks + 3 days
Schedule test now
Sample collection and transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
AF CytoMicroArray + FISH 21, AF CMA 750K + FISH 21, AF CMA High Resolution + FISH 21
Specialities
ObGyn, IVF, Fetal Medicine
Technology
CMA: The Affymetrix Cytoscan 750K Array includes 750,000 CNV markers with 550,000 unique non polymorphic probes and around 200,000 SNPs. Clinically significant CNVs of >100Kb reported. Data is analysed using Chromosome analysis suite (ChAS) software and interpreted using bioinformatic predictor tools, research publications and ACMG guidelines. The test does not detect balanced chromosomal translocations , small indels and point mutations. FISH: DNA probes (small molecules of DNA that are designed to hybridise with a particular section of the genome) are used detect specific complementary sequences on a chromosome. It is undertaken in situ on chromosomes spread on a slide and visualised by microscopy.
Conditions & Symptoms
High risk screening (Double marker, Quadruple Marker or NIPT) results, high risk for aneuploidy, bad obstetric history, parents carriers of translocations, history of Trisomy 21 or Down syndrome baby or fetus, ultrasound markers
Related Tests
Genetic Counselling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
750
2 weeks
Book now
Amniocentesis
Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy. Amniocentesis is an ultrasound guided sterile proceedure performed by experienced radiologits to retrive 20-30ml of the amniotic fluid from the womb. The fluid which contains fetal cells is used in the genetic lab to test for genetic abnormalities. It is done between 16-22 weeks of gestation. Amniocentesis proceedure is done at our central laboratory in Hyderabad. Prior appointment required. Call 9848041127 for details
7500
2 weeks
Book now
CVS Karyotyping
Karyotyping is a test performed on Chorionic Villi Sample (CVS) to identify fetal chromosomal numerical abnormalities (aneuploidy) and structural rearrangements such as inversions, insertions, translocations etc in the fetus.
8000
2 weeks
Book now

Frequently asked questions

What is Genetic Testing?
What are the uses of Genetic Testing?
What are the types of Genetic testing?
Are all genetic disorders hereditary?
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GeneTech is India’s leading genetics testing laboratory with the most comprehensive directory of genetic tests. We were established in Hyderabad in 1998, and have operations all over India.
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Book Counselling

GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.
GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.

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