Array46 750k test is an in-depht analysis to detect chromosomal alterations, CNVs and SNPs
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE212870
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The array46 750k study was performed in the DNA sample for mosaicism aneuploidy detection and loss or absence of heterozygosity. Samples include patients with phenotype associated with pigmentary mosaicism The array46 750k study was performed in the DNA sample to discard uniparental disomy (UPD) To detect chromosomal alterations, CNVs and SNPs
创建时间：
2022-11-17
