“…Numerous CNVs have been routinely identified using various genome analysis platforms, including single nucleotide polymorphism (SNP) genotyping platforms (Di Gerlando et al ., 2019), array comparative genomic hybridization (aCGH) (Zhang et al ., 2014) and next-generation sequencing (Xu et al ., 2017). These studies have been performed in humans (Altshuler et al ., 2010; Mills et al ., 2011), mice (Guryev et al ., 2008; Yalcin et al ., 2011), pigs (Wang et al ., 2013 a , 2014), horses (Doan et al ., 2013; Kader et al ., 2016; Corbi-Botto et al ., 2019), cattle (Jiang et al ., 2013; Yang et al ., 2017 a ), goats (Fontanesi et al ., 2010; Liu et al ., 2018; Zhang et al ., 2019) and chickens (Wang et al ., 2010). Over the past decades, significant progress has been made in mapping SNPs and insertions/deletions (Indels), the lengths of which are much smaller than those of CNVs, but there is less comprehensive annotation of CNVs (Pang et al ., 2010).…”