Variant DetailsVariant: esv2725496 Internal ID | 9959802 | Landmark | | Location Information | | Cytoband | 1q43 | Allele length | Assembly | Allele length | hg38 | 628 | hg19 | 628 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6773629, essv6816827, essv6738997, essv6766692, essv6844044, essv6756683, essv6700820, essv6750187, essv6914138, essv6697054, essv6789367, essv6714430, essv6769715, essv6972696, essv6750759, essv6933506, essv6871869, essv6764308, essv6961853, essv6793507, essv6859425, essv6720298, essv6670787, essv6918340, essv6878409, essv6736129, essv6669262, essv6874860, essv6955054, essv6864195, essv6804569, essv6675392, essv6847332, essv6742304, essv6853525 | Samples | SSM059, SSM008, SSM071, SSM027, SSM064, SSM065, SSM087, SSM050, SSM074, SSM088, SSM057, SSM092, SSM021, SSM029, SSM026, SSM089, SSM032, SSM003, SSM031, SSM001, SSM086, SSM066, SSM006, SSM085, SSM007, SSM078, SSM016, SSM053, SSM005, SSM091, SSM070, SSM043, SSM052, SSM063, SSM012 | Known Genes | ACTN2 | 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) | esv2725496
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 35 | Observed Complex | 0 | Frequency | n/a |
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