Variant DetailsVariant: esv1495197Internal ID | 12311634 | Landmark | | Location Information | | Cytoband | Xp22.13 | Allele length | Assembly | Allele length | hg38 | 70 | hg19 | 70 | hg18 | 70 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv4208997 | Samples | HuRef | Known Genes | NHS | Method | Sequencing | Analysis | | Platform | Sanger Sequencing | Comments | | Reference | Levy_et_al_2007 | Pubmed ID | 17803354 | Accession Number(s) | esv1495197
| Frequency | Sample Size | 2 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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