Supplementary_Table_1A_ CNVs_per_sample.tab
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资源简介：
Detailed list of copy number variants (CNVs) identified per individual in the studied family, including chromosomal coordinates, affected genes, CNV type (deletion or duplication), confidence level, and clinical interpretation focusing on relevance to enamel defects and amelogenesis imperfecta (AI).
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SciELO Data
创建时间：
2025-07-23
