CNSeq (500 KB Resolution)

Test Code
SLS165532
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What is CNSeq (500 KB resolution)?

CNSeq is an advanced alternative for chromosomal microarray analysis. This revolutionary technology can pick up any chromosomal abnormality utilizing NGS technology and provides superior accuracy in detecting Copy Number Variants (CNVs) compared to traditional cytogenetic methods. CNSeq offers the following features:

  • Detects CNVs and aneuploidies across the genome with a resolution of 500 Kb for both gains and losses
  • Offers uniform CNV calling capability
  • Capable of detecting low-level mosaicism

What abnormalities does CNSeq detect?

  • All aneuploidies (abnormal number of chromosomes)
  • Copy Number Variants (CNVs)
  • Structural variants

Who is CNSeq for?

  • Individuals with suspected chromosomal abnormalities
  • Individuals with intellectual disability or developmental delays
  • Individuals with congenital anomalies
  • Prenatal diagnosis of chromosomal abnormalities
Methodology: Low Pass Whole Genome Sequencing, NGS

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