Variant DetailsVariant: esv2758209Internal ID | 9633668 | Landmark | | Location Information | | Cytoband | 10p15.1 | Allele length | Assembly | Allele length | hg38 | 167673 | hg19 | 167673 | hg18 | 167676 | hg17 | 167676 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2759729 | Supporting Variants | essv14514, essv9028 | Samples | NA19202, NA19132 | Known Genes | ASB13, FAM208B | 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) | esv2758209
| Frequency | Sample Size | 270 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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