Variant DetailsVariant: nsv610538Internal ID | 16051261 | Landmark | | Location Information | | Cytoband | 8p22 | Allele length | Assembly | Allele length | hg38 | 10090 | hg19 | 10090 | hg18 | 10090 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv12014n54 | Supporting Variants | nssv1106891, nssv1106881, nssv1106897, nssv1106895, nssv1106885, nssv1106893, nssv1106886, nssv1106892, nssv1106890, nssv1106894, nssv1106887, nssv1106883, nssv1106896, nssv1106884, nssv1106882, nssv1106879, nssv1106889, nssv1106888, nssv1106880, nssv1106898 | Samples | | Known Genes | TUSC3 | 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) | nsv610538
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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