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NS = Not significant.
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创建时间：
2013-03-22
相关数据集
Array CGH analysis of human uveal melanomas. Array CGH analysis of human uveal melanomas
Primary uveal melanomas show multiple chromosomal aberrations. To identify genome variation in six human primary uveal melanomas, genome wide copy number variation (CNV) analyses were carried out in h
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Rare CNVs identified in 82 patients with pulmonary atresia.
P, pathogenic; UK, unknown; PP, potentially pathogenic.
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Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig5a]. Mus musculus
Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma
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Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Type 1 Diabetes Genetics Consortium (T1DGC) was formed to address issues of limited sample size and consistency of phenotyping that had limited genetic investigations on risk of type 1 diabetes (T1D).
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Table_3_Copy Number Variation Pattern for Discriminating MACROD2 States of Colorectal Cancer Subtypes.XLSX
Copy number variation (CNV) is a common structural variation pattern of DNA, and it features a higher mutation rate than single-nucleotide polymorphisms (SNPs) and affects a larger fragment of genomes
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