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Cortexa research tool·clinical·progenetix

Progenetix Cnv Search

Search for cancer biosamples with copy number variations (CNVs) in a specific genomic region. Combines disease filter with genomic coordinates to find samples with amplifications or deletions in genes of interest. Uses RefSeq chromosome accessions for coordinates. Example: searching for EGFR amplifications (refseq:NC_000007.14:55019017-55211628, DUP) in breast cancer (NCIT:C4017) returns 9 matching biosamples.

AvailableCortexa

Schema

JSON Schema the agent (or your API call) must match.

JSON · 39 lines · 1,177 chars

Examples (1)

Default Progenetix Cnv Search call

public-safeinput
JSON · 6 lines · 66 chars
Expected response keys: success

Anonymous-safe example. Rate-limited; no sign-in required.

Identifiers

Catalog ID
tu_Progenetix_cnv_search
Tool name
Progenetix_cnv_search
Added
2026-05-01 00:58Z
Tags
tooluniverse
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