1. Unmatched Resolution: Detects thousands of genetic conditions, microdeletions, and microduplications invisible under standard karyotyping.
2. Comprehensive Evaluation: Screens the entire genome in a single test, reducing the need for multiple diagnostic protocols.
3. Crucial Developmental Insights: Helps identify the genetic root causes of developmental delays, intellectual disabilities, and autism spectrum disorders.
4. Reproductive & Prenatal Clarity: Provides essential answers for couples experiencing recurrent pregnancy losses or abnormal ultrasound findings.
5. Expert Guidance Included: Every test is backed by a comprehensive post-report genetic counseling session to help you understand results and map out next steps.
🧬 Chromosomal Microarray Analysis Panels
Copy Number Variations (CNVs):
Detection of submicroscopic deletions and duplications across the genome
Chromosomal Anomalies:
Unbalanced translocations, aneuploidy detection
Regions of Homozygosity (ROH):
Identification of consanguinity and recessive disease risk regions
SNP Genotyping:
Allele-specific copy number analysis and zygosity assessment
Chromosomal Microarray Analysis (CMA) using Illumina SNP microarray platform. Detects copy number variations (CNVs), unbalanced translocations, and regions of homozygosity across the genome at high resolution. Processed in a NABL-accredited laboratory.