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SurePrint HD CGH Prenatal Research 2x105K Microarray

Agilent Technologies

Catalog Code: G5959AProduct Unit: 5 slides
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Designed and optimized by Baylor College of Medicine experts to target regions relevant to prenatal research. The CGH+SNP arrays also allow for the detection of copy neutral aberrations such as absence of heterozygosity (AOH) and uniparental disomy (UPD). Design ID = 20721

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