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nsv817445 - (obsolete)

  • Study:nstd37 (obsolete - ClinGen Laboratory-Submitted)
  • Variant Type:copy number variation
  • Method Type:Oligo aCGH
  • Submitted on:NCBI36 (hg18)
  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: Yes
  • Region Size:8,269,432
  • Description:the duplicated material is inserted into the q-arm of chromosome 1. Phenotype: minor congenital anomalies. PLEASE NOTE: The calls represented in this region now have equivalents in the study Clinical Structural Variants (nstd102). Please use the preferred nstd102 variant region accession for this variant; you can find it at top right under "Links to Other Resources" or in the mapping file provided here.
  • Publication(s):Miller et al. 2010
  • Replacement Description: Replaced nstd37 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
  • Replacement Variant: nsv3911051
This variant has been obsoleted and is no longer valid.
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