A full resolution version of this figure is available as
Figure 4—figure supplement 1—source data 1.(
a) Haplotypic representation of 1000 SNPs flanking the gap from 1546 imputed haploid chr11 genotypes from 773 cenhap-homozygous individuals. SNPs were filtered for MAC ≥ 35 and passing the
4gt_dco with a tolerance of 3. Minor alleles are shown in black. Assembly is gap indicated by the red line. Scaled chr11-specific α-satellite array size (AS) at left. Cenhap partitions at right; most common cenhap ‘3’, the cenhap with largest mean array size (‘4’) and an additional likely HuRef cenhap ‘5’ are highlighted. (
b) Box plots of the distributions of numbers of non-matching SNPs between HuRef and the indicated cenhap genotypes. The same 8816 SNPs as in
Figure 3 were genotyped in both the 1000 Genomes and HuRef. HuRef cenhap genotype is most likely 3_5 and does not involve the cenhap with the largest mean array size.