Microarray 750K (AF/CVS/CB/POC/PB) Test
Short Name: Microarray 750K
Also known as: Chromosomal Microarray Analysis, CMA 750K
Microarray 750K (AF/CVS/CB/POC/PB) Test test available at DNA Labs India for ₹24,000. Uses Microarray Analysis, Affymetrix Platform on Amniotic fluid/ Chorionic villi/Products of Conception/Cord blood/Peripheral blood samples. Results in 7-9 days. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The primary purpose of the Microarray 750K test is to identify genetic abnormalities that may be causing symptoms or health conditions. It is used for prenatal diagnosis, postnatal evaluation, and in cases of unexplained developmental issues. By detecting copy number variations and other chromosomal changes, it aids in accurate diagnosis, genetic counseling, and personalized treatment planning.
- Test Code
- 3093
- Price
- ₹24,000
- Sample Type
- Amniotic fluid/ Chorionic villi/Products of Conception/Cord blood/Peripheral blood
- Result Time
- 7-9 days
- Fasting Required
- No
- Method
- Microarray Analysis, Affymetrix Platform
Sample Collection
A doctor's prescription is required, except for cases involving surgery, pregnancy, or travel abroad. Discuss any concerns with your healthcare provider.
Method: Varies by sample type (e.g., venipuncture for blood, amniocentesis for AF)
Laboratory Analysis
Sample collection is performed by a trained professional. For blood, venipuncture is done; for amniotic fluid, amniocentesis is performed under ultrasound guidance.
Report Delivery
The sample is sent to the laboratory for analysis. Results are available in 7-9 days and can be accessed online or via email/WhatsApp.
Timeline: 7-9 days
Patient Instructions
About This Test
Who Should Get This Test
The primary purpose of the Microarray 750K test is to identify genetic abnormalities that may be causing symptoms or health conditions. It is used for prenatal diagnosis, postnatal evaluation, and in cases of unexplained developmental issues. By detecting copy number variations and other chromosomal changes, it aids in accurate diagnosis, genetic counseling, and personalized treatment planning.
How to Prepare
- Use appropriate container for sample type (Sterile Container or EDTA Vacutainer)
- Maintain cool pack during transport to preserve sample integrity
- Ensure sample is labeled correctly with patient details
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Microarray 750K is a comprehensive genetic test that aids in early diagnosis and management of genetic disorders, particularly in prenatal and postnatal settings, guiding clinical decisions and genetic counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Improperly labeled sample
Understanding Your Results
Normal
No pathogenic copy number variations detected, suggesting no major chromosomal abnormalities
Abnormal
Pathogenic CNV identified, which may be associated with genetic disorders; genetic counseling and further testing recommended
Variant of Uncertain Significance
CNV detected but clinical significance is unclear; correlation with clinical findings and family studies needed
If the test results are abnormal, if there are concerns about genetic disorders, or if you have a family history of genetic conditions, consult a geneticist or the referring physician for further evaluation and management.
Limitations
- ⚠Cannot detect single gene disorders
- ⚠May not identify balanced chromosomal rearrangements
- ⚠Variants of uncertain significance may be reported
Risks & Considerations
- ●For blood draw: minor bruising, pain, or infection at the puncture site
- ●For amniocentesis: small risk of miscarriage, infection, or amniotic fluid leakage
- ●For chorionic villus sampling (CVS): risk of miscarriage, infection, or limb defects in rare cases
Interfering Factors
- ●Sample contamination
- ●Improper sample handling
- ●Maternal cell contamination in prenatal samples
Compare With Similar Tests
| Test | Microarray 750K (AF/CVS/CB/POC/PB) | Karyotyping | FISH Test |
|---|---|---|---|
| Comparison | Microarray 750K (AF/CVS/CB/POC/PB) | Detects larger chromosomal abnormalities (e.g., aneuploidies), while microarray identifies smaller copy number variations genome-wide | Targeted test for specific chromosomal regions, whereas microarray provides comprehensive analysis across the entire genome |
Frequently Asked Questions
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₹7,371Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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