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cge12271-sup-0001-TableS1.docWord document31KTable S1. Summary informations of clinical features and general chromosome microarray analysis (CMA) detection of the prenatal fetuses in our study
cge12271-sup-0002-TableS2.docWord document32KTable S2. Evolution of single nucleotide polymorphism (SNP) arrays used in our report
cge12271-sup-0003-TableS3.docWord document48KTable S3. Common benign variants with an existing frequency of >5% in congenital malformation fetuses

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