GWAS results for dSVs (top) and vSVs (bottom). The x axis shows the genomic position on the human chromosomes (chromosomes 122) for both the top and bottom panels. The y axes in both panels show statistical significance as -log10[P] estimated using a linear mixed model by fastGWA. The plotted P values are not adjusted for multiple testing. The red horizontal lines indicate the study-wide significance cutoffs determined using the Bonferroni method: 3.00 x 10-11 for dSV and 2.65 x 10-11 for vSV associations. Significantly associated loci are highlighted in yellow and labelled with the nearby human gene and the corresponding species name.
