CHROMOSOMAL ARRAY CGH PLUS SNP, POC

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NABL Cap Accredited 

The Chromosomal Array CGH Plus SNP POC test provides high-resolution analysis of chromosomal copy number changes along with SNP-based detection of regions of homozygosity, uniparental disomy, and mosaicism. Metropolis Healthcare performs this advanced genomic test using state-of-the-art microarray technology to deliver comprehensive and accurate results. It is extremely useful in evaluating developmental disorders, congenital anomalies, and complex genetic conditions. When interpreted with clinical evaluation, it offers deep insight into genomic causes and guides further care.

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 17,640.00

Sample Type: POC

Fasting Not Required


Notes: C0247

Frequently Asked Questions (FAQ's):

What does the chromosomal array CGH plus SNP test include at Metropolis Healthcare?
It includes genome-wide copy number analysis plus SNP analysis for homozygosity and mosaicism.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-resolution microarray platforms and strict quality procedures.

Why is this test important?
It detects genetic abnormalities missed by routine karyotype and provides additional genomic information.

Who should take this test at Metropolis Healthcare?
Patients with developmental delay, dysmorphic features, unexplained anomalies, or suspected genetic disorders.

Do I need special preparation before the test?
No special preparation is required; a POC or blood sample is used as advised.

How long does it take to get results from Metropolis Healthcare?
Results are reported within the standard turnaround time for advanced genomic analysis.

Can this test detect all types of mutations?
It detects copy number and SNP-related changes but not all single-gene mutations; Metropolis Healthcare may suggest further testing.

How are results used by clinicians at Metropolis Healthcare?
Results support diagnosis, management planning, and genetic counselling for families.

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