Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting. - Mazzonetto, Patricia C.; Villela, Darine; da Costa, Silvia Souza; Krepischi, Ana C. V.; Milanezi, Fernanda; Migliavacca, Michele P.; Pierry, Paulo M.; Bonaldi, Adriano; Almeida, Luiz Gustavo D.; De Souza, Camila Alves; Kroll, José Eduardo; Paula, Marcelo G.; et al. (Annals of Human Genetics, 2024)