Variant DetailsVariant: nssv787257Internal ID | 15734527 | Landmark | | Location Information | | Cytoband | 12p13.31 | Allele length | Assembly | Allele length | hg38 | 85357 | hg19 | 85356 | hg18 | 85356 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv557261 | Supporting Variants | | Samples | | Known Genes | ATN1, CDCA3, DSTNP2, ENO2, GNB3, LEPREL2, LRRC23, RPL13P5, SPSB2, TPI1, USP5 | 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) | nssv787257
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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