loading . . . A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discovery Structural variants (SVs) can disrupt gene function and contribute to pathogenesis of rare disorders. Here, we created a genome-wide knockout dataset across 125,730 individuals with genome sequencing ... https://www.medrxiv.org/content/10.64898/2026.05.13.26352722v1
