Copy Number Variants of Uncertain Significance by Chromosome Microarray Analysis from Consecutive Pediatric Patients: Reevaluation Following Current Guidelines and Reanalysis by Genome Sequencing

作者：Wenjiao Li, Xiaolei Xie, Hongyan Chai, Autumn DiAdamo, Emily Bistline, Peining Li, Yuan Dai, James Knight, Abraham Joseph Avni-Singer, JoAnne Burger, Laura R. Ment, Michele Spencer‐Manzon, Hui Zhang, Jiadi Wen · 发表于：Genes · 年份：2025 · DOI：10.3390/genes16080874 · 被引用次数：2 · 研究领域：Genomic variations and chromosomal abnormalities、Genomics and Rare Diseases、Genetics and Neurodevelopmental Disorders

BACKGROUND: Copy number variants of uncertain significance (CNVus) from chromosome microarray analysis (CMA) presents unresolved challenges for clinical geneticists, genetic counselors, and patients. We performed a systematic reevaluation of reported CNVus and reanalysis of selected CNVus by whole genome sequencing (WGS) to assess the diagnostic value and clinical impact on CNVus reclassification. METHODS: We retrospectively reviewed 5277 consecutive pediatric cases by CMA from the Yale Clinical Cytogenetics Laboratory over a 13-year period. Reevaluation was performed on all reported CNVus following current ACMG/ClinGen guidelines. Reanalysis by WGS was applied to selected cases for reclassification of CNVus. RESULTS: A total of 567 CNVus from 480 cases were reported, which accounted for 9.1% of pediatric cases. A total of 4 CNVus in 4 cases (0.8%, 4/480) were reclassified to pathogenic/likely pathogenic CNVs (pCNVs/lpCNVs); while 23 CNVus in 23 cases (4.8%, 23/480) were reclassified to benign/likely benign CNVs (bCNVs/lbCNVs). The overall rate of reclassification was 5.6%. WGS performed on selected cases further defined breakpoints and ruled out additional causative genetic variants. CONCLUSIONS: The results from this study demonstrated the diagnostic value of periodic reevaluation of CNVus and reanalysis by WGS in an interval of 3-5 years and provided evidence to support standardized laboratory reevaluation and reanalysis.