Variant DetailsVariant: essv7112Internal ID | 9628988 | Landmark | | Location Information | | Cytoband | 19q13.2 | Allele length | Assembly | Allele length | hg38 | 392698 | hg19 | 392698 | hg18 | 392698 | hg17 | 392698 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758501 | Supporting Variants | | Samples | NA18537 | Known Genes | CEACAM8, LIPE-AS1, LOC100289650, PSG1, PSG10P, PSG3, PSG6, PSG7, PSG8 | 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) | essv7112
| Frequency | Sample Size | 270 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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