Variant DetailsVariant: nsv1005642Internal ID | 18748173 | Landmark | | Location Information | | Cytoband | 4q27 | Allele length | Assembly | Allele length | hg38 | 10992 | hg19 | 10992 | hg18 | 10992 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv5376n100 | Supporting Variants | nssv3639370, nssv3743090, nssv3639365, nssv3639366, nssv3639367, nssv3639369, nssv3639368 | Samples | | Known Genes | QRFPR | 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) | nsv1005642
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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