Variant DetailsVariant: dgv10454n54Internal ID | 20143878 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 102316 | hg19 | 102316 | hg18 | 102316 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv601887, nsv601903, nsv601902, nsv601885, nsv601905, nsv601891, nsv601877, nsv601888, nsv601906 | Samples | NINDS_192 | 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) | dgv10454n54
| Frequency | Sample Size | 17421 | Observed Gain | 21 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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