Variant DetailsVariant: dgv11063n54Internal ID | 20144487 | Landmark | | Location Information | | Cytoband | 6q27 | Allele length | Assembly | Allele length | hg38 | 208091 | hg19 | 208091 | hg18 | 208091 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv605398, nsv605400, nsv605409, nsv605441, nsv605397, nsv605399, nsv605393, nsv605396 | Samples | | Known Genes | FRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4 | 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) | dgv11063n54
| Frequency | Sample Size | 17421 | Observed Gain | 8 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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