Variant DetailsVariant: dgv10453n54 Internal ID | 20143877 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 106271 | hg19 | 106271 | hg18 | 106271 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv601882, nsv601899, nsv601904, nsv601871, nsv601909, nsv601907, nsv601869, nsv601883, nsv601875, nsv601920, nsv601897, nsv601890, nsv601908, nsv601914, nsv601879, nsv601872, nsv601873, nsv601918, nsv601874, nsv601900, nsv601901, nsv601876, nsv601913, nsv601881, nsv601919, nsv601898, nsv601912, nsv601884, nsv601870, nsv601911, nsv601910, nsv601878, nsv601921 | Samples | HGDP01208, HGDP01212, HGDP00445, HGDP00739, HGDP01250, HGDP00120, HGDP01237, HGDP00699, HGDP00878, HGDP00675, HGDP00945, HGDP01203, HGDP01290, HGDP01223, HGDP00753, HGDP01096, HGDP00830, HGDP00762, 1780862101_A, HGDP00689, HGDP00852, HGDP00771, HGDP00975, HGDP00733, HGDP00868, HGDP00656, HGDP00847, HGDP00920, HGDP00844, HGDP00110, HGDP01240, HGDP00927, 1780862094_A, HGDP00832, HGDP00876, HGDP01023, HGDP01251 | Known Genes | HCG26, HCP5, MICA | 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) | dgv10453n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 141 | Observed Complex | 0 | Frequency | n/a |
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