Sequencing data3 (CNV-seq)

This study aims to investigate copy number variations (CNVs) in children with abnormal brain development using high-resolution CNV-seq technology. The goal is to improve the diagnostic yield and expand the understanding of the genomic architecture associated with abnormal brain development. The dataset contributes valuable information for clinical genetics, pediatric neurology, and translational research on rare genetic disorders. Special statement: This sample is only for special patients