Variant DetailsVariant: esv2740394| Internal ID | 10324030 | | Landmark | | | Location Information | | | Cytoband | Xq23 | | Allele length | | Assembly | Allele length | | hg38 | 629 | | hg19 | 645 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv1321e201 | | Supporting Variants | essv6915525, essv6791085, essv6975753, essv6690957, essv6802964, essv6826941, essv6752010, essv6935284, essv6849988 | | Samples | SSM036, SSM073, SSM057, SSM021, SSM029, SSM086, SSM016, SSM080, SSM070 | | Known Genes | | | Method | Sequencing | | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | | Platform | Illumina HiSeq 2000 | | Comments | | | Reference | Wong_et_al_2012b | | Pubmed ID | 23290073 | | Accession Number(s) | esv2740394
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 9 | | Observed Complex | 0 | | Frequency | n/a |
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