MOESM2 of Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease

Additional file 2. “Frequencies of CNVs detected in our sample compared to those for controls from gnomAd and DDD”. Comparison of all the aberrations detected by aCGH in our study and the frequencies reported for controls in two databases.

补充文件2：《本研究样本中检测到的拷贝数变异（Copy Number Variation, CNV）频率与gnomAD、DDD对照人群的对比》。本内容对比了本研究通过阵列比较基因组杂交（array Comparative Genomic Hybridization, aCGH）检测到的全部染色体异常，与两个数据库中报道的对照人群异常发生频率。