Variant DetailsVariant: dgv6356n100Internal ID | 20157972 | Landmark | | Location Information | | Cytoband | 7p11.2 | Allele length | Assembly | Allele length | hg38 | 17548 | hg19 | 17548 | hg18 | 17548 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1031055, nsv1022735, nsv1026867, nsv1022907, nsv1024580, nsv1025115, nsv1034313, nsv1028509, nsv1035113 | Samples | | Known Genes | EGFR | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | dgv6356n100
| Frequency | Sample Size | 29084 | Observed Gain | 17 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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