Abstract
Information on chromosomal aberration rates in embryos derived from a young population, such as egg donors, is limited. PGT-A is the best predictive tool for embryo selection. It is most often offered to patients with advanced age, but with contradicting recommendations in younger patients. The objective was to evaluate the type and frequency of chromosomal aberrations in embryos derived from fresh young donor oocytes detected at NGS resolution of 10Mb and >30% mosaicism.
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