Variant DetailsVariant: esv2758504Internal ID | 9633963 | Landmark | | Location Information | | Cytoband | 19q13.33 | Allele length | Assembly | Allele length | hg38 | 274806 | hg19 | 274805 | hg18 | 274805 | hg17 | 274805 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2758767 | Supporting Variants | essv4577, essv374, essv4800, essv10047, essv17487, essv6589, essv4234, essv7000, essv23862, essv7093, essv3197, essv5456, essv23869, essv13837, essv13598 | Samples | NA18621, NA12814, NA18524, NA18603, NA19127, NA12762, NA07022, NA18537, NA19099, NA18974, NA18632, NA18971, NA18854, NA18612, NA18620 | Known Genes | CEACAM18, FLJ30403, FPR1, FPR2, HAS1, MIR125A, MIR99B, MIRLET7E, SIGLEC12, SIGLEC14, SIGLEC5, SIGLEC6, SPACA6P, SPACA6P-AS, ZNF175 | 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) | esv2758504
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 15 | Observed Complex | 0 | Frequency | n/a |
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