Human Gene Set: WP_16P1311_COPY_NUMBER_VARIATION_SYNDROME


Standard name WP_16P1311_COPY_NUMBER_VARIATION_SYNDROME
Systematic name M49222
Brief description 16p13.11 copy number variation syndrome
Full description or abstract  
Collection C2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP5502
Related gene sets  
External links https://www.wikipathways.org/pathways/WP5502
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Source species Homo sapiens
Contributed by WikiPathways
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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NCI-60 cell lines (National Cancer Institute)

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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Show members (show 29 source identifiers mapped to 29 genes)
Version history 2025.1.Hs: First Introduced.

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