Variant DetailsVariant: dgv10348n54 Internal ID | 20143772 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 47614 | hg19 | 47614 | hg18 | 47614 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv601273, nsv601280, nsv601287, nsv601345, nsv601305, nsv601279, nsv601355, nsv601328, nsv601323, nsv601281, nsv601354, nsv601324, nsv601295, nsv601290, nsv601286, nsv601282, nsv601276, nsv601335, nsv601293, nsv601320, nsv601333, nsv601270, nsv601275, nsv601288, nsv601363, nsv601289, nsv601347, nsv601364, nsv601292, nsv601327, nsv601346, nsv601362, nsv601274, nsv601358, nsv601321, nsv601352, nsv601351, nsv601379, nsv601356, nsv601306, nsv601294, nsv601297, nsv601325, nsv601326, nsv601285, nsv601283, nsv601296, nsv601322 | Samples | | Known Genes | HCG4B, HLA-H | 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) | dgv10348n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 93 | Observed Complex | 0 | Frequency | n/a |
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