E-MTAB-6820 - Copy number variants analysis of heterotaxy syndrome patients with congenital heart defects

Status
Released on 24 May 2018, last updated on 25 May 2018
Organism
Homo sapiens
Samples (63)
Array (1)
Protocols (5)
Description
To identify the molecular causes of heterotaxy syndrome patients with congenital heart defects, an Affymetrix CytoScan HD array was used to identify possible pathogenic CNVs in 63 patients. A total of 59 samples passed initial quality control.
Experiment types
genotyping by array, pathogenicity design
Contact
MIAME
PlatformsProtocolsVariablesProcessedRaw
Files
Links