Variant DetailsVariant: essv18448Internal ID | 9616389 | Landmark | | Location Information | | Cytoband | 2p11.2 | Allele length | Assembly | Allele length | hg38 | 723923 | hg19 | 796319 | hg18 | 723923 | hg17 | 723923 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2757815 | Supporting Variants | | Samples | NA11831 | Known Genes | LINC00152, LOC285074, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2, PLGLB1, PLGLB2 | 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) | essv18448
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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