Variant DetailsVariant: nsv1017570Internal ID | 18760104 | Landmark | | Location Information | | Cytoband | 8p21.2 | Allele length | Assembly | Allele length | hg38 | 575222 | hg19 | 575222 | hg18 | 575222 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3685373 | Samples | | Known Genes | CHMP7, ENTPD4, LOC100507156, LOC254896, LOC286059, LOC389641, LOXL2, R3HCC1, RHOBTB2, SLC25A37, TNFRSF10A, TNFRSF10B, TNFRSF10C, TNFRSF10D | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | nsv1017570
| Frequency | Sample Size | 29084 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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