Additional file 2: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

Recurrent pathogenic/likely pathogenic CNVs detected by array-CGH in 36 children with ID/DD, ASD and MCA. (XLSX 14 kb)本数据集收录了通过阵列比较基因组杂交（array-based Comparative Genomic Hybridization, array-CGH）在36例伴智力障碍/发育迟缓（Intellectual Disability/Developmental Delay, ID/DD）、孤独症谱系障碍（Autism Spectrum Disorder, ASD）及多发性先天畸形（Multiple Congenital Anomalies, MCA）的儿童中检测到的复发性致病性/可能致病性拷贝数变异（Copy Number Variations, CNVs）。（XLSX 14 kb）