Variant DetailsVariant: nsv516646Internal ID | 15097253 | Landmark | | Location Information | | Cytoband | 19p13.3 | Allele length | Assembly | Allele length | hg38 | 35272 | hg19 | 35272 | hg18 | 35272 | hg17 | 35272 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv680239, nssv680883, nssv655651, nssv677472, nssv693678, nssv687548, nssv658752, nssv670935, nssv657535, nssv672733, nssv685991, nssv669846, nssv673447, nssv685893, nssv673238 | Samples | | Known Genes | SBNO2 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516646
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 15 | Observed Complex | 0 | Frequency | n/a |
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