Additional file 3 of Rare copy-number variants as modulators of common disease susceptibility

Additional file 3: Supplemental Tables. Table S1. Disease epidemiology. Table S2. Covariate selection and probe prefiltering. Table S3. Genomic inflation of genotypic Fisher test p-values. Table S4. Genome-wide significant CNV-GWAS associations. Table S5. BMI adjustment for possibly confounded CNV-disease associations. Table S6. CNV region characteristics. Table S7. Impact of the CNV burden on disease risk. Table S8. Disease variance explained by the CNV burden.