MOESM1 of Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants

Additional file 1: Table S1. Coordinates of the de novo SV breakpoint junctions detected in the 39 individuals by WGS. Table S2. List of external data sources used in this study. Table S3. Phenotype information of the 39 included patients with de novo SVs. Table S4. Candidate driver genes detected for each included patient. Table S5. Fusion genes detected in the patients by RNA sequencing. Table S6. Candidate driver genes detected in patients’ cohorts. Table S7. Detected de novo copy number variants in 154 patients of the diagnostics cohort.