Variant DetailsVariant: essv6988896Internal ID | 12636144 | Landmark | | Location Information | | Cytoband | 3q12.2 | Allele length | Assembly | Allele length | hg38 | 100001 | hg19 | 100001 | hg18 | 100001 | hg17 | 100001 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2751970 | Supporting Variants | | Samples | SPC_102 | Known Genes | GPR128, TFG | Method | SNP array | Analysis | | Platform | Affymetrix Mapping 250K Nsp SNP Array | Comments | | Reference | Pinto_et_al_2007 | Pubmed ID | 17911159 | Accession Number(s) | essv6988896
| Frequency | Sample Size | 771 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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