<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE4nnn/GSE4659/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Genome variation profiling by genome tiling array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE4659</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>AML genome hybridization to HG44A</name><description>CGH analysis was conducted for AML blasts with Agilent HG44A arrays. Keywords: disease state analysis</description><dates><publication>2007/03/01</publication></dates><accession>GSE4659</accession><cross_references><GSM>GSM105160</GSM><GSM>GSM105161</GSM><GSM>GSM105168</GSM><GSM>GSM104772</GSM><GSM>GSM104773</GSM><GSM>GSM105166</GSM><GSM>GSM105167</GSM><GSM>GSM104771</GSM><GSM>GSM105164</GSM><GSM>GSM105165</GSM><GSM>GSM105162</GSM><GSM>GSM105163</GSM><GSM>GSM104787</GSM><GSM>GSM105159</GSM><GSM>GSM104786</GSM><GSM>GSM105157</GSM><GSM>GSM104783</GSM><GSM>GSM104784</GSM><GSM>GSM105158</GSM><GSM>GSM104781</GSM><GSM>GSM105155</GSM><GSM>GSM105156</GSM><GSM>GSM104782</GSM><GSM>GSM105153</GSM><GSM>GSM105154</GSM><GSM>GSM104780</GSM><GSM>GSM104778</GSM><GSM>GSM104779</GSM><GSM>GSM104776</GSM><GSM>GSM104777</GSM><GSM>GSM104774</GSM><GSM>GSM104775</GSM><GPL>2873</GPL><GSE>4659</GSE><taxon>Homo sapiens</taxon><PMID>[17361228]</PMID></cross_references></HashMap>