Extended Data Fig. 1: Distribution of aneuploid chromosomes across embryos.
From: Common variation in meiosis genes shapes human recombination and aneuploidy
Of all tested embryos, 70.25% were called as euploid, 20.49% exhibited aneuploidy affecting a single chromosome, and 9.26% exhibited more complex abnormalities affecting multiple chromosomes, including 1.08% exhibiting whole-genome gain and 0.23% exhibiting whole-genome loss or genome-wide uniparental isodisomy.
