Variant DetailsVariant: nsv546815Internal ID | 15987538 | Landmark | | Location Information | | Cytoband | 1p22.1 | Allele length | Assembly | Allele length | hg38 | 1117 | hg19 | 1117 | hg18 | 1117 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv367n54 | Supporting Variants | nssv719121, nssv719101, nssv719120, nssv719097, nssv719119, nssv719103, nssv719118, nssv719108, nssv719107, nssv719100, nssv719124, nssv719110, nssv719123, nssv719112, nssv719109, nssv719125, nssv719122, nssv719098, nssv719114, nssv719102, nssv719111, nssv719115, nssv719099, nssv719117, nssv719116, nssv719104, nssv719106, nssv719113, nssv719105 | Samples | | Known Genes | TGFBR3 | 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) | nsv546815
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
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