Variant DetailsVariant: nsv569801Internal ID | 16010524 | Landmark | | Location Information | | Cytoband | 15q23 | Allele length | Assembly | Allele length | hg38 | 238 | hg19 | 238 | hg18 | 238 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv844334, nssv844356, nssv844350, nssv844348, nssv844336, nssv844352, nssv844347, nssv844349, nssv844330, nssv844360, nssv844357, nssv844345, nssv844346, nssv844337, nssv844342, nssv844338, nssv844354, nssv844328, nssv844329, nssv844339, nssv844343, nssv844333, nssv844351, nssv844353, nssv844341, nssv844361, nssv844326, nssv844327, nssv844332, nssv844325, nssv844324, nssv844344, nssv844358, nssv844355, nssv844340, nssv844359, nssv844335, nssv844331 | Samples | | Known Genes | MAP2K5 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv569801
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 38 | Observed Complex | 0 | Frequency | n/a |
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