Variant DetailsVariant: esv1584074Internal ID | 12400509 | Landmark | | Location Information | | Cytoband | Xq11.1 | Allele length | Assembly | Allele length | hg38 | 8536574 | hg19 | 8536952 | hg18 | 8536952 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv3829597 | Samples | HuRef | Known Genes | ACRC, AMER1, AR, ARHGEF9, ARR3, ASB12, AWAT1, AWAT2, BCYRN1, CXCR3, CXorf49, CXorf49B, CXorf65, DGAT2L6, DLG3, EDA, EDA2R, EFNB1, FAM155B, FOXO4, FRMD8P1, GDPD2, GJB1, HEPH, IGBP1, IL2RG, INGX, ITGB1BP2, KIF4A, LAS1L, LINC00269, LINC00891, LOC100132741, LOC92249, MED12, MIR1468, MIR223, MIR676, MSN, MTMR8, NLGN3, NONO, OGT, OPHN1, OTUD6A, P2RY4, PDZD11, PJA1, RAB41, SLC7A3, SNX12, SPIN4, STARD8, TAF1, TEX11, VSIG4, YIPF6, ZC3H12B, ZC4H2, ZMYM3 | Method | Sequencing | Analysis | | Platform | Sanger Sequencing | Comments | | Reference | Levy_et_al_2007 | Pubmed ID | 17803354 | Accession Number(s) | esv1584074
| Frequency | Sample Size | 2 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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