Variant DetailsVariant: nsv511485Internal ID | 15504224 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 67213 | hg19 | 67213 | hg18 | 67213 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv626102 | Samples | 1 | Known Genes | OR4C11, OR4P4, OR4S2 | Method | SNP array | Analysis | Analysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array | Platform | GPL8882 | Comments | | Reference | Arlt_et_al_2011 | Pubmed ID | 21212237 | Accession Number(s) | nsv511485
| Frequency | Sample Size | 1 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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