MOESM2 of Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease
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https://figshare.com/articles/dataset/MOESM2_of_Copy_number_variations_in_candidate_genomic_regions_confirm_genetic_heterogeneity_and_parental_bias_in_Hirschsprung_disease/11158586
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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.
创建时间：
2019-11-25
