Variant DetailsVariant: esv2758431Internal ID | 9633890 | Landmark | | Location Information | | Cytoband | 16q22.3 | Allele length | Assembly | Allele length | hg38 | 252406 | hg19 | 252406 | hg18 | 252406 | hg17 | 252406 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2758656 | Supporting Variants | essv16547, essv5255, essv6177, essv13136, essv12323, essv11731, essv7194, essv4229, essv1995, essv13888, essv4793, essv16421, essv16822, essv2982, essv13087, essv18232 | Samples | NA18603, NA18547, NA19138, NA18949, NA19210, NA19205, NA18981, NA19154, NA18532, NA12057, NA19102, NA18854, NA18852, NA18624, NA19139, NA18620 | Known Genes | CLEC18B, GLG1, LOC283922, PSMD7 | 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) | esv2758431
| Frequency | Sample Size | 270 | Observed Gain | 8 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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