Variant DetailsVariant: nssv2995908Internal ID | 15234768 | Landmark | | Location Information | | Cytoband | 19q13.31 | Allele length | Assembly | Allele length | hg38 | 174337 | hg19 | 173584 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv483005 | Supporting Variants | | Samples | | Known Genes | CEACAM16, CEACAM19, CEACAM22P, IGSF23, MIR4531, PVR | Method | BAC aCGH | Analysis | | Platform | Spectral Genomics 2600 BAC array | Comments | | Reference | Iafrate_et_al_2004 | Pubmed ID | 15286789 | Accession Number(s) | nssv2995908
| Frequency | Sample Size | 39 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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