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. 2019 Apr 26;212(2):469–487. doi: 10.1534/genetics.119.302232

Figure 6.

Figure 6

Genotypes of N2 females (left) and males (right) at informative sites between the PWK/PhJ Y chromosome and the PWK/PhJ X or WSB/EiJ X haplotypes under the PWK/PhJ Y-linked duplication. The same set of parental inbred strain controls is shown in both top panels. Genotype calls are color-coded as homozygous for the mm10 reference allele (HOM_A1), heterozygous (HET), or homozygous for the alternate allele (HOM_A2). Missing calls (NA) are shown in gray. Recombinant individuals shown with red arrowheads. SNV, single-nucleotide variant.