17q12 Knowledge Basedeletion syndrome · static snapshot
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Phenotype expansion kidney and urinary tract 1 supporting source confidence 97% novelty 90%

New observation reported: To identify such novel alterations and to discover the underlying genes, we performed comparative genomic hybr…

A source describes a new or expanded observation: “To identify such novel alterations and to discover the underlying genes, we performed comparative genomic hybridization on a set of 22 human pancreatic cancer cell lines, using cDNA microarrays measuring approximately 26,000 human genes (thereby providing an average mapping resolution of <60 kb).”

More phenotype expansion

How this was derived

Flagged by novelty language (“for the first time”, “expands the phenotype”, …) in pubmed.

Generated 2026-11-13, last changed yesterday. Dedup key expansion:72f35f. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

Array-based comparative genomic hybridization identifies localized DNA amplifications and homozygous deletions in pancreatic cancer. peer_reviewed · published 2005-06-01 · live page
To identify such novel alterations and to discover the underlying genes, we performed comparative genomic hybridization on a set of 22 human pancreatic cancer cell lines, using cDNA microarrays measuring approximately 26,000 human genes (thereby providing an average mapping resolution of <60 kb).

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
Array-based comparative genomic hybridization identifies localized ... pubmed 2005-06-01 yesterday 1.00