Variant DetailsVariant: nsv556236Internal ID | 15996959 | Landmark | | Location Information | | Cytoband | 11q22.3 | Allele length | Assembly | Allele length | hg38 | 4354 | hg19 | 4354 | hg18 | 4354 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2155n54 | Supporting Variants | nssv783412, nssv783401, nssv783402, nssv783410, nssv783404, nssv783403, nssv783409, nssv783395, nssv783396, nssv783394, nssv783406, nssv783399, nssv783416, nssv783407, nssv783413, nssv783397, nssv783408, nssv783415, nssv783411, nssv783400, nssv783414, nssv783398, nssv783405 | Samples | | Known Genes | GUCY1A2 | 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) | nsv556236
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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