E-MTAB-6820 - Copy number variants analysis of heterotaxy syndrome patients with congenital heart defects
Released on 24 May 2018, last updated on 25 May 2018
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.
genotyping by array, pathogenicity design