Chromosomal Microarray Blood
Chromosomal microarray analysis of blood helps identify genetic abnormalities, including deletions and duplications, that may be linked to developmental disorders, autism, and congenital anomalies. It provides a more detailed genetic picture compared to traditional karyotyping.
No special preparations needed
- Specimen
- Clinical History
- Deletion
- Duplication
- Autosomal Aneuploidies
- Sex Chromosome Aneuploidies
- Interpretation
Test code
6041M
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 2 ML |
| Others (fx) | Others | 2 ML |
Specimen stability information
Edta Whole Blood, Others (Fx)
Collection instructions
EDTA Whole Blood/ Products Of Conception (Poc) / Amniotic Fluid / Cvs In Sterile Saline + Clinical History [For Prenatal Samples Af & Cvs - Duly Filled Trf + Clinical History. Consent Form- G With Pnd Registeration No. Is Mandatory. Specimen Should Reach Us In 24Hrs In Sterile Condition.
Specimen rejection criteria
Test run frequency
'
Turn around time
15 Working Days
Performing locations
Department
- Cytogenetics
CPT and Loinc codes
Package price
₹16500
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₹16500