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Array-CGH

The LCG has different array resolutions in order to identify Copy number variations (CNV) and detection of loss of heterozygosity. This diagnosis can be done on pre-natal and post-natal samples.

Array-CGH 60K oligos

Array-CGH 180K oligos

Array-CGH 400K (300.000 oligos+100.000 SNPs)

Technique:
  • Array Comparative Genomic Hybridization - Array-CGH
Method:Comparative genome hybridization
Products:
  • DNA
  • Fetal DNA
  • Human Genomic DNA
  • Tumor biopsies
Certification:Certificação NP EN ISO 9001:2015
Access types
  • Físico
  • Enviado por correio
Access mode
  • Paid
Geographical availability
  • Europe
Languages
  • Português
  • Inglês
Tags:
Service provided byCytogenetics and Genomics Laboratory