Variant DetailsVariant: nsv10810 Internal ID | 15499087 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 123951 | hg19 | 123951 | hg18 | 123951 | hg17 | 123951 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv14145, nssv14706, nssv14826, nssv14017, nssv15853, nssv14298, nssv13847, nssv15128, nssv14042, nssv15211, nssv15158, nssv15181, nssv16560, nssv13522, nssv15219, nssv13987, nssv13974, nssv15189, nssv14796, nssv13552, nssv14102, nssv13886, nssv13856, nssv14338, nssv14308, nssv13817, nssv14268, nssv14464, nssv14566, nssv14596, nssv14115, nssv15867, nssv16364, nssv13001, nssv14328, nssv15981, nssv16011, nssv14494, nssv13582, nssv13970, nssv15897, nssv14583, nssv14015, nssv13787, nssv16523, nssv13855 | Samples | NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA18972, NA18552 | Known Genes | HCG4B, HCG9, HLA-A, HLA-H | Method | Oligo aCGH | Analysis | Statistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2 | Platform | Agilent-015686 Custom Human 244K CGH Microarray | Comments | | Reference | Perry_et_al_2008 | Pubmed ID | 18304495 | Accession Number(s) | nsv10810
| Frequency | Sample Size | 31 | Observed Gain | 25 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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