Additional file 2 of Insertion variants missing in the human reference genome are widespread among human populations

Table S1. Sensitivity and false discovery rate of InserTag, ANISE, MindTheGap and PopIns on simulated data. Table S2. Validation of InserTag by fosmid-clone confirmed insertion variants. Table S3. Number of paired insertion-tags traced to target genomes. Table S4. Phenotype-associated SNPs with high linkage disequilibrium with non-reference insertion variants. Table S5. Ratio of high linkage disequilibrium between phenotype-associated SNPs and non-reference insertion variants. (XLSX 38.7 kb)