Variant DetailsVariant: nssv958897Internal ID | 15906167 | Landmark | | Location Information | | Cytoband | 3p25.3 | Allele length | Assembly | Allele length | hg38 | 149331 | hg19 | 149331 | hg18 | 149331 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv589648 | Supporting Variants | | Samples | | Known Genes | CIDECP, CRELD1, EMC3, EMC3-AS1, FANCD2, IL17RC, IL17RE, JAGN1, LOC401052, PRRT3, PRRT3-AS1 | 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) | nssv958897
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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