Supplementary Material from Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects

Supplementary Figure and Tables. Supplementary Figure 1: Gene ontologies for genes identified in 35 CNVs of interest; Supplementary Table 1: Rare coding region CNVs detected in the 225 patient heterotaxy cohort; Supplementary Table 2: Genes identified in rare coding region CNVs detected in the 225 patient heterotaxy cohort; Supplementary Table 3: Rare copy number variants at loci previously associated with CHD; Supplementary Table 4: Rare CNVs identified at loci associated with known microdeletion / duplication syndromes but not heterotaxy or CHD.