Variant DetailsVariant: esv2747719 Internal ID | 9982003 | Landmark | | Location Information | | Cytoband | 1p34.1 | Allele length | Assembly | Allele length | hg38 | 1244 | hg19 | 1244 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6666919, essv6910080, essv6917472, essv6921754, essv6877131, essv6729652, essv6803709, essv6967968, essv6784898, essv6695932, essv6946522, essv6853277, essv6669443, essv6756573, essv6883273, essv6738836, essv6769556, essv6733505, essv6744967, essv6710616 | Samples | SSM059, SSM024, SSM065, SSM087, SSM009, SSM042, SSM002, SSM028, SSM047, SSM018, SSM017, SSM006, SSM015, SSM005, SSM055, SSM095, SSM052, SSM049, SSM030, SSM012 | Known Genes | RNF220 | 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) | esv2747719
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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