Variant DetailsVariant: dgv6755n54Internal ID | 20140179 | Landmark | | Location Information | | Cytoband | 2p22.3 | Allele length | Assembly | Allele length | hg38 | 1637 | hg19 | 1637 | hg18 | 1637 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv581323, nsv581314, nsv581319, nsv581320, nsv581324, nsv581318, nsv581311, nsv581322, nsv581312, nsv581326, nsv581315, nsv581316, nsv581329, nsv581327 | Samples | | Known Genes | RASGRP3 | 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) | dgv6755n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 126 | Observed Complex | 0 | Frequency | n/a |
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