Variant DetailsVariant: nsv514795Internal ID | 15466429 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 396 | hg19 | 396 | hg18 | 396 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2819540, nssv2819529, nssv2819537, nssv2819536, nssv2819532, nssv2819533, nssv2819541, nssv2819535, nssv2819531, nssv2819538, nssv2819539, nssv2819530, nssv2819534 | Samples | NA19122, NA21391, NA19123, NA19235, NA19210, NA19103, NA19097, NA19101, NA19095, NA21425, NA19211, NA18500, NA21581 | Known Genes | FOPNL | Method | Oligo aCGH | Analysis | ADM2 threshold = 5 | Platform | Agilent Eichler Human CNP 180K v3.0 | Comments | | Reference | Campbell_et_al_2011 | Pubmed ID | 21397061 | Accession Number(s) | nsv514795
| Frequency | Sample Size | 2366 | Observed Gain | 13 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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