A-C. Deletion allele frequencies and observed sharing of alleles across populations, displayed for deletions discovered in the CEU, YRI, and JPT+CHB population samples in terms of stacked bars. D. Allele frequency spectra for deletions intersecting with intergenic (blue), intronic (yellow), and protein-coding sequences (red).

A. Distribution of SVs on chromosome 10 (“chr10”). Above the ideogram, colored bars indicate SV formation mechanisms (same color scheme as in B and C); bar lengths relate to the logarithm of SV size. Below the ideogram, bar lengths are directly proportional to allele frequencies. Arrows indicate an SV hotspot near the centromere underlying mainly VNTR, and several hotspots near the telomeres underlying mainly NAHR events. B. Enrichment of SVs inferred to be formed by the same formation mechanism for different genomic window sizes. Displayed is an enrichment of nearby, non-overlapping SVs formed by the same mechanism relative to an SV set where mechanism assignments are shuffled randomly. C. SV hotspots are mostly dominated by a single formation mechanism. Colored bars depict numbers of SV hotspots in which at least 50% of the variants were inferred to be formed by a single formation mechanism. The average abundance of NAHR-classified SVs in NAHR hotspots was 70% (compared with 77% for VNTR-hotspots; 69% for NH). The gray bar (“mixed”) corresponds to SV hotspots with no single mechanism dominating.

A. Schematic depicting the different modes (i.e., approaches) of sequence based SV detection we used. The RP approach assesses the orientation and spacing of the mapped reads of paired-end sequences14,15 (reads are denoted by arrows); the RD approach evaluates the read depth-of-coverage25,26; the SR approach maps the boundaries (breakpoints) of SVs by sequence alignment28,29; the AS approach assembles SVs30,31,32. B. Integrated pipeline for SV discovery, validation, and genotyping. Colored circles represent individual SV discovery methods (listed in Supplementary Table 1), with modes indicated by a color scheme: green=RP; yellow=RD; purple=SR; red=AS; green and yellow=methods evaluating RP and RD (abbreviated as ‘PD’). C. Example of a deletion, previously associated with BMI35, identified independently with RP (green), RD (yellow), and SR (red) methods. Grey dots indicate position and mapping quality for individual sequence reads. Targeted assembly confirmed the breakpoints detected by SR.

A. Breakpoint junction homology/microhomology length plotted as a function of SV size for SVs originally identified as deletions compared to a human reference. Dots are colored according to the SVs’ classification as deletions, insertions/duplications, or “undetermined” relative to inferred ancestral genomic loci. Gray lines mark groups of SVs likely formed by a common formation mechanism. The diagonal highlights tandem duplications (and few reciprocal deletion events), in which the length of the duplicated sequence correlates linearly with the length of the longest breakpoint junction sequence identity stretch. The ellipses indicate MEIs, i.e., Alu (~300 bp) and L1 (~6 kb) insertions, associated with target site duplications of up to 28 bp in size at the breakpoints. The horizontal group corresponds mostly to NH-associated deletions with <10 bp microhomology at the breakpoints. The remaining (ungrouped) SVs comprise truncated MEIs, VNTR expansion and shrinkage events, as well as NAHR-associated deletions and duplications. B. Relative contributions of SV formation mechanisms in the genome. Numbers of SVs are displayed on the outer pie chart and affected base pairs on the inner. Left panel: SVs classified as deletions relative to ancestral loci. Right panel: SVs classified as insertions/duplications. C. Size spectra of deletions classified relative to ancestral loci. D. Size spectra of insertions/duplications.

A. Deletion size-range ascertained by different modes of SV discovery. Three groups are visible, with AS and SR, PD and RP, as well as RD and ‘RL’ (RP analysis involving relatively long range (≥1 kb) insert size libraries, resulting in a different deletion detection size range compared to the predominantly used <500kb insert size libraries), respectively, ascertaining similar size-ranges. Pie charts display the contribution of different SV discovery modes to the release set. Outer pie = based on number of SV calls; inner pie = based on total number of variable nucleotides. Of note, not all approaches were applied across all individuals (see Supplementary Table 2). B. Sensitivity and FDR estimates for individual deletion discovery methods based on gold standard sets for individuals sequenced at high (NA12878) and low-coverage (NA12156), respectively. All depicted estimates are summarized in Supplementary Tables 3, 4, 6. Vertical dotted lines correspond to the specificity threshold (FDR≤10%). C. Breakpoint mapping resolution of three deletion discovery methods (the respective method names are in Supplementary Table 2). The blue and red histograms are the breakpoint residuals for predicted deletion start and end coordinates, respectively, relative to assembled coordinates (here assessed in low-coverage data). The horizontal lines at the top of each plot mark the 98% confidence intervals (labeled for each panel), with vertical notches indicating the positions of the most probable breakpoint (the distribution mode).