Variant DetailsVariant: nssv1150485Internal ID | 15534085 | Landmark | | Location Information | | Cytoband | 2q13 | Allele length | Assembly | Allele length | hg38 | 96389 | hg19 | 96389 | hg18 | 96389 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv582687 | Supporting Variants | | Samples | NINDS_271 | Known Genes | LINC00116, NPHP1 | 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) | nssv1150485
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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