Variant DetailsVariant: esv2760065Internal ID | 9635524 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 112550 | hg19 | 112549 | hg18 | 112549 | hg17 | 112549 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2758405 | Samples | NA18502, NA11829, NA19204, NA18855, NA19131, NA19130, NA19159, NA19194, NA19205, NA19208, NA19154, NA18853, NA19101, NA19132, NA10856, NA19206, NA18501, NA19211, NA18506, NA18620 | Known Genes | MPG, NPRL3, POLR3K, RHBDF1, SNRNP25 | Method | BAC aCGH | Analysis | Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd). | Platform | Agilent | Comments | | Reference | Redon_et_al_2006 | Pubmed ID | 17122850 | Accession Number(s) | esv2760065
| Frequency | Sample Size | 270 | Observed Gain | 20 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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