Variant DetailsVariant: nsv602064Internal ID | 16042787 | Landmark | | Location Information | | Cytoband | 6p21.32 | Allele length | Assembly | Allele length | hg38 | 19144 | hg19 | 19144 | hg18 | 19161 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv10476n54 | Supporting Variants | nssv1053804, nssv1053805, nssv1053806, nssv1053803 | Samples | | Known Genes | C4A, C4B, C4B_2, STK19, TNXA, TNXB | 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) | nsv602064
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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