Molecular karyotyping (Array CGH) of fetal remains (pregnancy loss)
GenoLife
Delivery time
No especificado
Sample
No especificado
796,00€
This analysis can identify numerical chromosomal abnormalities, structural imbalances
Genome-wide rearrangements and copy number changes, covering regions of known clinical importance (recognized microduplication/microdeletion)
syndromes), pericentromeric and subtelomeric regions, and the genomic backbone. It uses a custom-designed Illumina single nucleotide polymorphism (SNP) array. This array contains more than 630,000 SNP markers spanning both coding and non-coding sequences of the human genome. The average spatial resolution between probes is 4.5 kb.
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VenuLife + Thrombopanel + Polycystic Ovary Syndrome
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