a, The power of discovery within the main data set for SNPs and indels identified within an overlapping sample of 284 genomes sequenced to high coverage by Complete Genomics (CG), and against a panel of >60,000 haplotypes constructed by the Haplotype Reference Consortium (HRC)9. To provide a measure of uncertainty, one curve is plotted for each chromosome. b, Improved power of discovery in phase 3 compared to phase 1, as assessed in a sample of 170 Complete Genomics genomes that are included in both phase 1 and phase 3. c, Heterozygote discordance in phase 3 for SNPs, indels, and SVs compared to 284 Complete Genomics genomes. d, Heterozygote discordance for phase 3 compared to phase 1 within the intersecting sample. e, Sensitivity to detect Complete Genomics SNPs as a function of sequencing depth. f, Heterozygote genotype discordance as a function of sequencing depth, as compared to Complete Genomics data.