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Validation of CNV Assay by array-CGH analysis. A) Trisomy of chromosome 7, but not EGFR amplification (probe position at +0.40), in BT314. B) Complete loss of chromosome 14q in BT314 (probe position at -0.40/-0.60); C)EGFR amplification in primary tumor BT418 (probe position at +0.60).
