WormBase Tree Display for Variation: WBVar00091258

WBVar00091258 Evidence: Paper_evidence: WBPaper00029073
  Name: Public_name: WBVar00091258
    Other_name: niDf237(V)
  Sequence_details: SMap: S_parent: Sequence: CHROMOSOME_V
    Flanking_sequences: ACAATCTTCCTGTTTGACGACTGTGAGCTC GTCGAGTGCTTGTCTTGTACGCGAATCTGA
    Mapping_target: CHROMOSOME_V
    CGH_deleted_probes: AGCCTGCGCCATCAAGGTCCGATTGTCTCGGTGTGGTATTCTCCTTGTAA TCAAAGGACTCGTATCCTCGATCGGACCCTTCCAATTCATCCGATCCATC
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850
    Laboratory: VC
    Person: WBPerson427
    Detection_method: Oligo Array CGH
    Status: Live
  Affects: Gene (19)
    Transcript (12)
    Pseudogene: Y17D7B.5
      F11D11.18
      F11D11.19
      F11D11.16
      F11D11.15
      F11D11.11
      F11D11.17
  Reference: WBPaper00029073
  Remark: Flanking sequences represent the nearest array oligo sequences present in the deletion chromsome on the basis of fluorescence ratio. These should not be considered hard breakpoints in the absence of actual sequence data. Original data available on-line at http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE6294.
  Method: CGH_allele