Variant DetailsVariant: nssv1143261Internal ID | 15649761 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 102700 | hg19 | 102700 | hg18 | 102700 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv615411 | Supporting Variants | | Samples | | Known Genes | C9orf114, ENDOG, LOC100506100, TBC1D13, ZER1 | 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) | nssv1143261
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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